The development of antidiabetic drugs with complementary mechanisms of acti
on appears more and more necessary in order to achieve durable glycaemic co
ntrol in type 2 diabetes. By inhibiting in a reversible way the hydrolysis
of disaccharides and the ultimate steps of the digestion of dietary polysac
charides, alpha-glucosidase inhibitors reduce postprandial blood glucose mi
se in diabetics. This therapeutic class, limited in Europe until recently t
o acarbose, has been enlarged with the marketing of miglitol, whose pharmac
okinetic properties might lead to better long term tolerance. The improveme
nt of glycaemic control obtained with alpha-glucosidase inhibitors is now b
etter evaluated and appears similar whatever the combinations with other an
tidiabetic drugs, including insulin. The role of alpha-glucosidase inhibito
rs in the overall therapeutic strategy of type 2 diabetes and their benefit
on the evolution of long term complications remains to be clarified (C) 19
99 Elsevier, Paris.